P, Q and R in the above-mentioned sequence of reactions are respectively:
1. | |
2. | |
3. | |
4. |
The molecule among the following that has the hybridization from left to right atoms is:
1.
2.
3.
4.
The correct statement regarding the comparison of staggered and eclipsed conformations of ethane is:
1. | The eclipsed conformation of ethane is more stable than staggered conformation because eclipsed conformation has no torsional strain. |
2. | The eclipsed conformation of ethane is more stable than staggered conformation even though the eclipsed conformation has a torsional strain. |
3. | The staggered conformation of ethane is more stable than eclipsed conformation because staggered conformation has no torsional strain. |
4. | The staggered conformation of ethane is less stable than eclipsed conformation because staggered conformation has a torsional strain. |
X and Y in the above-mentioned reaction are respectively:
1. X = 2–Butyne; Y = 3–Hexyne
2. X = 2-Butyne; Y = 2-Hexyne
3. X = 1-Butyne; Y = 2-Hexyne
4. X = 1-Butyne; Y = 3–Hexyne
HCl with an alkene X reacts in accordance with Markovnikov’s rule to give 1-Chloro-1-methylcyclohexane. The structure of alkene (X) is:
1. | 2. | ||
3. | (1) and (2) | 4. |
2,3-dimethyl-2-butene can be prepared by heating which of the following compounds with a strong acid?
1.
2.
3.
4.
The reaction of C6H5CH =CHCH3 with HBr produces:
1. | \(C_{6} H_{5} \underset{Br}{\underset{\left|\right.}{CH}} CH_{2} CH_{3} \) |
2. | \(C_{6} H_{5} CH_{2} \underset{Br}{\underset{\left|\right.}{CH}} CH_{3} \) |
3. | \(C_{6} H_{5} CH_{2} CH_{2} CH_{2} Br \) |
4. |
When subjected to ozonolysis, which compound results in the formation of the given molecule?
1. | 2. | ||
3. | 4. |
Given compounds are as follows:
(I) | (II) | ||
(III) |
The enthalpy of hydrogenation of these compounds will be in the order as-
1. | I > II > III | 2. | III > II > I |
3. | II > III > I | 4. | II > I > III |
The product(s) that are formed when the given compound is treated with Br2 in the presence of FeBr3 are:
1. | 2. | ||
3. | 4. |